Where the angle comes from

The organ that was nobody's neighbour

Twenty-one of the thirty wrecked offsets remove an organ that lies on neither contact chain through the tip. The reading that explains the other nine has nothing to say about them, and the honest thing is to say so rather than to widen the definition until it does.

Worth reading first: The organ that was taken away · Counting the spirals · A head is a set of points.

The family that lost a member is the family that survives, on every row where the question can be asked. That is nine rows of thirty. This essay is about the other twenty-one, and it is mostly an argument for leaving them alone.

Every wrecked offset, and whose neighbour was removed. Each row is a stem that never repaired, with the family of the organ that was taken and the family that survived. An organ five places back on a stem counted at 5 and 8 spirals lies on the tip's five-chain, so the question can be asked there; an organ four places back lies on neither chain and it cannot. Of 30 wrecked offsets in the census, 9 remove a member of exactly one family and 21 remove a member of neither. On every one of the 9 the family that lost a member is the family left standing, which is the opposite of what the reading predicted.
Fig. 1 Every wrecked offset with the column added. Most rows say “neither chain”, and those are the subject here.

An organ k places back from the tip lies on the tip’s own p-chain exactly when p divides k. On a stem counted at 5 and 8 spirals the answerable offsets are five and eight. Four, six and seven are not multiples of either, so the organ removed there is not a neighbour of the tip along any chain the counter names, and the reading has no purchase.

The proportion is not an accident of this lattice. Inside a front of depth q there are q offsets, and the multiples of p or q among them number about q/p + 1 — so the answerable fraction falls as the counted numbers grow apart and rises as the front deepens. On a 5/8 stem it is two offsets in eight. The twenty-one are what that arithmetic looks like summed over five lattices, and they would be twenty-one whatever the physics turned out to be. That is worth knowing before treating the gap as a finding about the rule rather than about the census’s shape.

A prediction and its opposite, scored on the same rows. The reading under test said the family whose member was removed is the one that breaks. Scored across every wrecked offset where the removed organ lies on exactly one contact chain — 9 of 30, the other 21 being silent because the organ lies on neither — it is right no times and its opposite is right nine. A chain that loses a member does not stop existing: the organs above the hole are still spaced at that lag and the rule that placed them is still minimising the same sum, while the other chain has lost the organ its members were positioned against.
Fig. 2 The reading and its opposite, scored on the rows where either can be asked, with the count of rows where neither can printed beneath.

What those rows do

They wreck, and they keep a contact family like every other row. Offset four on a 5/8 stem keeps the five at almost every rise on its rung; offsets six and seven keep the eight. So there is structure — it is exactly the structure the offset rule describes — and the point is that the lost-member reading is not what produces it.

The one exception is instructive. At the finest rise on the rung, offset four keeps the eight rather than the five, which is the row that changes hands along the rung. It is a silent row by the divisibility test and it is also the single row in the whole sweep whose answer depends on the rise. Whatever is happening at the offsets that belong to no chain is evidently more sensitive to the geometry than what happens at the offsets that do — which is a hint about where to look, and is as far as a hint should be pushed.

Which family survives, along the 5/8 rung. The family a wrecked stem keeps, at every offset that wrecks and every rise on one rung. A counter shown any of these stems returns 5 and 8 spirals, at all twelve rises, so nothing in the pair distinguishes the columns. The cells say otherwise: at an offset of 4 the stem keeps the 5-family at the coarse end of the rung and the other one at the fine end. The offsets that wreck at all grow from 1 to 5 as the rise falls, because the front deepens, and the extra offsets are the ones that keep the larger number. So the rule stated over the offset alone is a rule with the rise left out of it.
Fig. 3 Those offsets along a whole rung, where four keeps the smaller family and six and seven keep the larger.
Which lag survives, at every lattice and every offset. A row for each of twelve lattices and a column for each offset an organ is removed at, with the lag whose hop survived written in the cell. 30 cells never repair. The lag left standing is one of the two contact families at 29 of them, and at 17 it is the second shortest step on the lattice rather than the shortest, which is what refuses the reading that a rule holds its nearest neighbours. The ringed cells are the five the offset rule gets wrong. Two lattices carry no cells at all because no single removal wrecks them.
Fig. 4 And the census the offset rule was scored on, with its five failures marked.

The offset rule covers them by arithmetic: four is no further back than five, so the five survives; six and seven are beyond it, so the eight does. That is a correct description of what happens and it says nothing about why an organ that is nobody’s neighbour should have any effect at all.

And it should have an effect — that part is not mysterious. The rule minimises a sum over every organ already placed, not over a chain, so a removal anywhere inside the front changes the sum the next organ is placed against whether or not the removed organ was anybody’s nearest neighbour. What is mysterious is why the outcome should sort itself into two families when the disturbance does not respect chains at all. The restriction to two families is the strongest result this thread has, and the twenty-one are where it is least explained.

The next organ moves for the last 8, and for no others. One row per organ removed, counted back from the tip of a stem at a rise of 0.013 whose counted pair is 5 and 8. Removing any of the last 8 moves the next organ by 4.9° to 164.1°; removing an older one moves it by at most 0.70°, which is under the azimuth grid. The boundary is at 8, and 8 is the larger parastichy number — so the experiment counts the spirals without measuring an angle.
Fig. 5 That it has an effect is not in doubt: the displacement a removal causes is large at every offset inside the front, chain member or not.
Take away the organ four places back, and the next one goes into the hole. The last 30 organs of a stem at a rise of 0.013, unrolled. The open circle is the organ removed — four places before the tip. The ring at the top is where the rule puts the next organ with every organ present; the filled mark beside it is where the rule puts it with that one missing. The two are 164.1° apart, against a local spacing of 41°, and the vacancy itself is 172.7° from the undisturbed answer. Nothing else differs between the two runs: same rise, same history, same rule.
Fig. 6 The intervention at one of the silent offsets, four places back, which is nobody’s chain neighbour and wrecks the stem anyway.

The extension that is available, and why it is not taken

There is an obvious way to make the reading cover everything, and it is worth setting out precisely so that its cost is visible.

Chains are not a property of the tip. The organ four places back lies on the five-chain through the organ one place above the tip, and on the eight-chain through some organ further down; every organ lies on both chains through somebody. So one could say: the family that survives is the one whose chain through the nearest affected organ lost a member — and with the right choice of reference organ, every row becomes answerable.

A cell's neighbours are its spiral families. Left: part of a 700-point golden, 137.508° head, with every contact between two cells drawn and coloured by the difference between the two nodes' placement indices. Right: the share each difference takes, across all 1459 contacts between interior cells. They are the parastichy numbers — 34, 55, 21, 89, 13, 8 — and the pair a person would count is 34 and 55. The six sides Euler forces are shared out among four of them, 5.64 edges per cell.
Fig. 7 Why the extension is tempting: every organ touches members of both families, so a chain can be found through anything.
A stem unrolled: 180 nodes at 136.78° with a rise of 0.013 circumferences. The counter is shown these coordinates and the circumference, and finds 5 parastichies one way and 8 the other. The faint strips left and right are the same stem: a family leaving one edge re-enters at the other.
Fig. 8 And the arrangement it would be read off, where five places back and eight places back are the two organs directly below the tip.

That is exactly the shape of a free parameter. “The nearest affected organ” is a choice, and there are several defensible ones — the tip, the newest organ whose placement moved, the organ closest to the hole in the arrangement rather than in the sequence. Each gives a different assignment on the twenty-one rows, and with three choices and twenty-one rows it would be surprising if none of them scored well.

This collection has been caught by exactly that shape before. Four different definitions of how deep the rule looks disagree about the size of the neighbourhood by a factor of ten, and the choice between them was a free parameter nobody had varied. A reading that needs a reference organ chosen after the rows are known is a reading whose score is about the choosing.

Four ways to count the rule's neighbourhood, and one ordering. How many organs the placement rule is looking at, as its falloff exponent is swept from 1.5 to 6, by three different definitions. Counting the organs that carry half the profile gives 33, 12, 3, 2, 1. Counting the organs that carry nine tenths gives 182, 120, 30, 8, 3. Counting the organs that carry the weighted mean lag gives 68, 45, 21, 14, 11. They disagree about the size of the neighbourhood by a factor of 10 — the widest moves by 61 times across the sweep and the narrowest by 6.1 — and every one of them falls as the exponent rises. So no choice among them changes which rule is the deeper, and no redefinition can turn a result about the depth around.
Fig. 9 The worked example of that hazard: three summaries of one quantity, disagreeing by a factor of ten and each defensible.

What would earn the extension

A reference organ chosen for a reason rather than for a score, and stated before the rows are looked at.

There is a candidate with a reason behind it. The rule places each organ at the minimum of a sum over the organs already there, so the organ whose placement the removal actually disturbed most is a measurable thing, not a choice: it is the one whose azimuth moves furthest between the cut run and its control.

The newest member of the front is the weakest. For every cell of the design whose rung boundary is inside the range, how far the next organ moves when the organ exactly as many places back as the larger parastichy number is removed — the offset that arrived when the stem entered this rung — against how far below that boundary the stem sits. Each line is one lattice on one branch. The horizontal line is the threshold that decides whether an offset counts as felt, and the one cells below it are the one whose front reads one offset short. Nothing is a different kind of thing: the boundary is a step everywhere, and near the top of a rung its last stair is shallow.
Fig. 10 The measured gradient that makes such a quantity available: the strength of the response at the newest member of the front.
On a rung the response is a run of offsets; near a transition it has a hole. One row per rise, from 0.032 at the top to 0.005 at the bottom, and one column per offset: the organ one place back at the left, 14 places back at the right. A cell is filled where removing that organ moves the next organ by more than 2.5°, and empty where it does not. On a rung the filled cells are a run from one to the larger parastichy number — 5, 8, 13 at the pairs shown on the left. Every rise shown here is in the middle of its rung, so every row is a run and nothing past it is felt — what happens between the rungs is a separate matter.
Fig. 11 And the range over which a removal is felt at all, which bounds where any reference organ could be.

Defining the reference organ that way is falsifiable in the way the tip version is: compute the most-disturbed organ, ask which chains it lies on, and score the prediction on all thirty rows at once. If it holds on the twenty-one as well as the tip version holds on the nine, the reading is the account. If it does not, it is dead, and it dies on rows chosen by a rule rather than by hand.

One wrecked stem, lag by lag — golden, rise 0.013, organ 4 back. How much each lattice hop moves from organ to organ in a stem that never repaired after a single removal, over its last 120 organs. The lag-one hop is the divergence itself and it swings by 65 degrees. The lag-5 hop swings by 0.11 degrees and sits 0.09 degrees from where the undisturbed stem put it, so that one family of the original lattice is still standing organ by organ. Its multiples inherit the same steadiness and nothing else comes within a factor of twenty. The block of angles this stem repeats has a period of 5, which is the surviving lag and not a coincidence.
Fig. 12 One row read by lags rather than by neighbours, which is how the survivor is defined and how any such prediction would be scored.

That measurement does not exist yet. It is one column, like the last one, and this essay’s job is to say what the column has to contain rather than to guess what it will say.

There is a reason to expect it to be interesting rather than merely confirmatory. The organ whose placement moves most is not always adjacent to the hole: the response to a removal is not a smooth falloff along the sequence but a pattern with structure in it, because the sum being minimised is over positions in the arrangement rather than over indices. So the most-disturbed organ could easily lie several places from the cut, on chains the cut itself is not on, and the prediction it generates need not agree with the offset rule at all. A reading that can disagree with the incumbent is worth computing; one that cannot is bookkeeping.

Three things the twenty-one already rule out

They are not a ragged remainder. They are the offsets strictly between the two counted numbers, plus those below the smaller one, and they behave consistently: below the smaller number they keep the smaller family, between the two they keep the larger. Whatever is happening is systematic.

How many offsets wreck, along the 5/8 rung. The count of offsets that never repair, at each rise on one rung. It runs from 1 at the coarse end to 5 at the fine end, while a counter returns 5 and 8 spirals at every one of them. The front — the run of recent organs at which a removal is felt at all — deepens as the rise falls, so there are simply more places a cut can land and fail to heal. That is the mechanism under the grid: the offsets that appear at the fine end are the ones beyond the smaller contact number, and those are the ones that keep the larger family.
Fig. 13 Where those offsets come from: the front deepening down a rung, which is what brings the between-the-numbers offsets into existence.

They are not explained by step length. The shortest-hop reading is a coin flip along a rung, and restricting it to these twenty-one does not improve it.

Which offsets give short hops, at a rise of 0.013. The two lowest points are at 5 and 8, and those are the parastichy numbers. Offset 1 is high because a hop of one node is at least the rise, which is what makes a stem easier to count than a disc.
Fig. 14 The step lengths at one rise, which do not separate the silent rows from the answerable ones.
The two contact steps change places inside the 5/8 rung. Measured at every rise on one rung, where a counter returns 5 and 8 spirals throughout. The settled divergence slides from 136.6406 to 137.8672 degrees. The ratio of the two contact steps falls to 1.0131 at a rise of 0.016 and the ordering changes hands at 0.015: above it the shorter step belongs to the 5-family and below it to the 8-family. Neither quantity is available to a counter, which is shown positions and reports a pair, and both of them move while that pair does not.
Fig. 15 And the ordering of those two steps across a rung, which reverses without the answers at these offsets changing.

And they are not an artefact of one lattice. The twenty-one are spread across five lattices on two branches, and the pattern is the same on both. Nor are they concentrated at one end of the front: they run from offsets below the smaller counted number to offsets between the two, and both groups behave consistently with the offset rule while being invisible to the lost-member one. If the silent rows were all crowded against the deepest edge of the front — where a removal is barely felt and the wreck is marginal — the gap could be dismissed as a boundary effect. They are not, and it cannot.

The same rule, the same rise, two lattices, two fronts. How many organs back a single removal is still felt, on a stem seeded onto the golden lattice and on one seeded onto the Lucas lattice, at seven rises. Everything but the seed is identical at each rise — the rule, the spacing, the heights, the azimuth grid — and the two fronts differ at every one of them. Which branch has the wider front changes hands four times going down the range, so no function of the rise gives the column. The golden branch carries 5/8 at four of these rises, across a factor of two in the rise, and its front is eight at all four.
Fig. 16 The two branches carry fronts of different depth at the same rise, and the silent offsets appear on both.
The block is one of the two numbers, and not always the smaller. Every lattice a single organ was removed from, one row each: golden, rise 0.013 carrying 5/8; golden, rise 0.008 carrying 5/8; golden, rise 0.005 carrying 8/13. The two open ticks on each line are that lattice's own parastichy numbers; the filled dots are the blocks the stems that never recovered settled into, one per offset that failed. The claim this table was built to test is that the block is the smaller of the two, which held at the two rises it was first measured at. It does not hold here: 5/8 gives 5 and 8. What survives is weaker and still worth something — every filled dot but 1 sits on one of that row's own ticks, so the orbit carries a count of the lattice it was cut from, and which of the two it carries is decided by the offset rather than by the pattern.
Fig. 17 The same rows in the quantity that first raised the question: the period of the motif a wrecked stem repeats.

Why a gap is worth publishing

A collection that only published the nine would be publishing a rule with a hidden domain, and hidden domains are how a fit becomes folklore. The nine are a strong result — a stated prediction, refuted backwards, replaced by its opposite at every row — and they cover three tenths of the census. Both halves of that sentence are load-bearing.

The failure mode is specific and this thread has already produced one instance of it. “The rule keeps its shortest hop” was stated as a rule and scored at twelve of twenty-nine, which sounds like a refutation and was really a statement about a census whose sampling correlated the ordering with the pair. A reading quoted without its domain is a reading whose next reader cannot tell which of those two situations they are in. Writing the twenty-one down is what makes the nine quotable.

There is a sharper reason than tidiness, and it comes from setting this essay’s count beside the one the offset rule carries.

The offset rule is right at twenty-five of thirty. The lost-member reading is right at nine of nine — and on those nine the two return the same answer, because an organ lying on the tip’s p-chain is also, in the offset rule’s arithmetic, a cut landing at or beyond p. So the five rows that defeat the offset rule cannot be among the nine. All five of them are inside these twenty-one.

That changes what the gap is. It is not a region where a good rule has yet to be extended. It is the region where the best available rule does all of its failing, and where the mechanism that might explain those failures is silent by construction. The nine rows the two accounts share carry no information whatever about their disagreement.

It also prices the cheap strengthening described above. Sweeping finer rungs adds answerable rows, and answerable rows are rows where the two accounts already agree, so thirty or forty of them would raise the lost-member reading’s count without touching one row that separates it from the arithmetic it is meant to explain. As a check against coincidence the strengthening is real; as a test between the two readings it is worth nothing.

That test has to be run on these twenty-one, which is the whole case for treating them as the subject rather than the leftovers. A census built to settle the thread would sample offsets that are nobody’s neighbour on purpose, at several rises, and ask whether the answers there follow anything at all — because if they follow nothing, the offset rule’s five failures are not failures of a rule but the visible edge of a domain nobody has drawn.

Agreement between two windows happens only on a slow enough shoot. Five stems at each of four rates and five disturbances, each read through two overlapping windows of 250 internodes. A filled mark is agreement — both windows reported the same pair; a half mark is a disagreement; a small mark is one window reporting and one refusing; an open mark is silence. Agreement appears 0 times in 25, 1 times in 25, 14 times in 25, 14 times in 25 at 130, 250, 400, 700 nodes per rung, and the two rates it is almost absent from are the two at which a rung is no longer than the window.
Fig. 18 The general shape of a scored comparison: several stated readings, one table, and every score reported rather than the winner alone.
Every open question here needs under 28 specimens. The sample size at which each comparison reaches 80 per cent power at a 5 per cent false-positive rate, from the exact binomial rather than a normal approximation. The census question — do plants show consecutive Fibonacci pairs far more often than the geometry does — needs 4: 14.7% is the share of divergence angles giving a consecutive Fibonacci pair at a fine rise; 90% is what a grown history gives.
Fig. 19 And the form the same caution takes when the claim is to be made about real plants rather than runs.

There is also a practical reason. The twenty-one can be reduced without any new idea, simply by sweeping finer rungs: at 8/13 the answerable offsets are eight and thirteen, at 13/21 they are thirteen and twenty-one, so a deeper front makes a larger fraction of its offsets chain members. The gap is partly a property of which rungs have been swept.

That reduction has a ceiling, and it is worth computing before anybody sets off. Within a front of depth q the multiples of p and q stay a roughly fixed fraction as the ladder is climbed, because p and q grow together — the answerable share tends to about one offset in three rather than to all of them. So finer rungs make the nine into thirty or forty and never into everything. The silent rows are a permanent feature of asking the question this way, not a backlog to be worked off, and any account that finishes the thread has to speak to them directly. Sweeping along a rung adds rows of both kinds at once, which is the cheapest way to find out whether the two behave differently under the one variable the census never moved.

Every transition as the rise falls. The pair climbs 1/2 → 2/3 → 3/5 → 5/8 → 8/13. Consecutive transitions are 0.381, 0.382, 0.382 of the previous rise — 1/φ² is 0.3820.
Fig. 20 Where those rungs are, and how few of them any ablation census has visited.
The band that never heals is what two fixed edges leave over. Each row is one rung. A stem is grown to 400 organs, one organ is removed, and the stem is followed for 300 more. A filled mark is an offset the stem recovers from, with the number of organs it took printed above it; an open ring is an offset it never recovers from. At the 3/5 rung, a front of 5, every offset heals. At the 5/8 rung, a front of 8, the offsets 4, 5 never heal. At the 8/13 rung, a front of 13, the offsets 4, 6, 7, 8, 9 never heal. What is the same at every rung is the two edges: the first three offsets heal, and so do the last few of the front. What is left in the middle is the band, and it widens because the front does.
Fig. 21 With the caution attached: whether a stem is wreckable at all is a property of where it sits on that ladder.

Where this leaves it

The thread now has a mechanism-shaped statement that is right wherever it applies, an arithmetic rule that covers nearly everything and explains nothing, and a clean boundary between them. That is a better position than a single rule at twenty-five of thirty, because the boundary is where the next measurement goes.

The block a wrecked stem settles into is the count it was cut from. A stem is cut in the middle of its front and followed for 300 organs. It does not come back to its lattice; what it does instead is repeat a fixed sequence of divergences exactly, to the resolution of the azimuth grid. Each row shows that sequence twice over, one bar per organ, drawn to the same scale. At the 5/8 rung the sequence is five angles long and advances -36.1° per block; At the 8/13 rung the sequence is eight angles long and advances 22.5° per block. Every block is the smaller number of the pair that was cut, so the second attractor carries the first one's count — and every precession is one part in twice the block, which makes each of these a two-jugate arrangement with 10 and 16 rows.
Fig. 22 What all of these rows decide in the end: the length of the motif a wrecked stem repeats, which is the family that was kept.
A second cut moves the next organ, and does not move the boundary. Every pair of organs that can be taken out of a settled stem at a rise of 0.013, where the pattern is 5/8. A row is the offset of the nearer organ removed, counted back from the tip; a column is how many further places back the second one sits. The shade is how far the next organ ends up from where it would have been, from under a degree in the palest cells to a half-turn in the darkest. The run of shaded rows ends at 8, which is the larger parastichy number, and every row below it is blank across the whole width — the largest displacement anywhere past the front is 1.41°. So the nearer of the two organs decides whether the removal is felt at all, and the second one, wherever it is put, cannot make the pattern notice an organ it was not going to notice.
Fig. 23 And the table one rise produces, with the offset along one axis and the second removal along the other.

Nothing here is a placeholder for a result that is coming. It is a statement of what twenty-one rows do not currently support, written down so that the next person to score a reading over this census — including a later version of this collection — has to score it over all thirty.

The general form is worth keeping. A reading that applies to a subset defined by the data rather than by the question is a reading with a domain, and the domain has to be stated in the same breath as the score. Here the subset is defined by divisibility, which is at least a property of the arrangement and not of the outcome — so the nine are a fair test rather than a selection. Had the subset been “the rows where the reading works”, there would be no result at all, and the distance between those two situations is exactly one sentence of bookkeeping that is easy not to write.

What links here

Computed from the collection, not written here: the essays that point at this one.

Shares its objects with

Essays that name at least two of the same things, and that neither author linked.

  • The front deepens down a rung — both name ablation, claim testing, control, honest limits, lattice, lattice offset, measurement, negative result, parastichy pair, the placement rule, rigid hop, rung
  • One rise per rung is a sample — both name claim testing, control, falsifiability, honest limits, lattice, measurement, negative result, parastichy pair, rung, underdetermination
  • The hop that survived — both name ablation, falsifiability, honest limits, lattice, lattice offset, measurement, parastichy pair, the placement rule, rigid hop, rung
  • Two accounts of one number — both name ablation, claim testing, honest limits, lattice, measurement, negative result, parastichy pair, the placement rule, rung, underdetermination
  • What a count cannot decide — both name claim testing, control, honest limits, lattice, measurement, negative result, parastichy, parastichy pair, rung, underdetermination
  • A period that is not a count — both name ablation, falsifiability, honest limits, lattice, lattice offset, measurement, parastichy, parastichy pair, rigid hop

Named objects

A flat tag is an object no other essay names yet.

AblationClaim testingControlFalsifiabilityHonest limitsLatticeLattice offsetMeasurementNegative resultParastichyParastichy pairThe placement ruleRigid hopRungUnderdetermination